Canonical Allele Identifier: PA2742023428
Gene: SLC51B HGNC NCBI

Linked Data

ClinVar Variation Id: 2772761
ClinVar RCV Id: RCV003576841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849190.2:p.Met24Thr
CA392871113
NM_178859.4:c.71T>C